Polyaromatic hydrocarbons (PAHs) are widely spread pollutants in the environment, including soil and water. Anthracene (anth) and phenanthrene (phen) pose severe health impacts on human lives due to their carcinogenic nature by increasing cancer risk to the skin, lungs, and bladder. Fluorescence spectroscopy is a promising , efficient and straightforward tool for characterizing these trace PAHs in water. Therefore, the current work provides a detailed insight into the fluorescence properties of anth and phen in water. The fluorescence EEMs (excitation-emission matrices) of anth showed emissions at 380 nm, 400 nm, and 425 nm with single excitation at 250 nm, whereas phen showed two emissions < 380 nm, at 350 nm and 365 with single excitation at 250 nm. Then the theoretical EX/EM wavelengths were calculated by DFT and CIS-B3LYP for these compounds in water. The environmental effect of pH variation on fluorescence EEM shows a significant difference in fluorescence intensity without changing in peak locations, with highest fluorescence intensity at neutral pH than acidic and alkaline. Furthermore, the theoretical pH effect was described for the first time by simulating the protonated (+ 1), deprotonated (-1) and neutral molecules in water at the DFT level of theory. The variation in simulated oscillator strengths was similar in trend with the experimental fluorescence intensity of these compounds. The HOMO-LUMO were calculated to obtain the energy gap, molecular softness, molecular hardness, electronic potential and electrophilicity of anth and phen. To find the fluorophore contribution, the fluorescence of homogeneous mixture of both isomers was analyzed, which showed an enhanced fluorescence intensity of anth by 12-20%, whereas a decrease of 9-14% was observed in phen. This study describes that the fluorescence technique could be a fast and easy method to distinguish and identify PAHs isomers (anth and phen) in water.

In the last two decades, awareness grew on the matter of the impact of environment on human health. Contaminants sorbed onto soil and settled dust can be ingested and thus represent a hazard, particularly to young children, who play on the ground and bring their hands and objects to their mouth. Metal(loid)s and polycyclic aromatic hydrocarbons (PAHs) are of concern as they are both carcinogenic to humans and ubiquitous in outdoor environments. The present study aims to assess the total and bioaccessible fractions of PAHs and metal(loid)s present in settled dust of four preschools located in industrial, urban, and suburban areas. On the one hand, children\'s incremental life cancer risks (ILCR) were calculated according to ingestion pathway. On the other hand, the genotoxicities of the bioaccessible dust-bonded contaminants were determined on gastric cells. PAH concentrations ranged from 50.9 to 2267.3 ng/g, and the bioaccessible fraction represented 10.7% of the total in average. Metal(loid) concentration ranged from 12,430 to 38,941 µg/g, and the mean bioaccessibility was of 40.1%. Cancer risk ranged from 2.8.105 to 8.6.105, indicating that there is a potential cancer risk for children linked to the ingestion of settled dust. The inorganic bioaccessible fraction induced little DNA (< 20%TailDNA) and chromosomal damages (30% increase in micronuclei), whereas the organic bioaccessible fraction induced higher DNA (17-63%TailDNA) and chromosomal damages (88% increase in micronuclei). Such experimental approach needs to be deepen, as a tool complementary to cancer risk calculation, since the latter only lays on a set of targeted contaminants with known toxicity values.

An investigation was conducted into the dynamic behavior of two polyaromatic hydrocarbon (PAH) semi-volatile organic compound (SVOC) naphthalene (NAP) and benzo [ghi]perylene (BghiP) in air and on various surfaces including glass, dust, and polyurethane foam (PUF) to understand their interaction with different media. A confocal fluorescence microscope and an infrared microscope were employed to detect and monitor the concentration-, time-, and temperature-dependent changes of the aromatic NAP and BghiP species on the surfaces. Infrared two-dimensional mapping of the vibrational characteristic peaks was used to track the two PAHs on the surfaces. Gas chromatography-mass spectrometry (GC-MS) was employed to measure the gaseous concentrations. The sorption of NAP and BghiP on the surfaces was estimated using Arizona desert sand fine (ISO 12103-1 A2) dust and organic contaminant household (SRM 2585) dust. The surface-to-air partition coefficients of NAP and BghiP were estimated on the different surfaces of glass, dust, and PUF. Molecular dynamic simulations were performed on dust surfaces based on the Hatcher model to understand the behavior of NAP and BghiP on dust surfaces. The Weschler-Nazaroff model was introduced to predictPAH film accumulation on the surfaces, providing a better understanding of PAH interaction with different environmental media. These findings could contribute to developing effective strategies to mitigate the adverse impact of PAHs on the environment and human health.

This study aimed to assess the impact of the eThekwini Municipality reforestation project on the quality of the soil within the reforestation sites, and water from the nearby rivers (White and Black Mhlasini Rivers) situated at the reforested Buffelsdraai area in KwaZulu-Natal, South Africa. This was the first evaluation of the effect of reforestation on the reduction of selected organic pollutants to be conducted in this area. The sixteen polyaromatic hydrocarbons analysed are on the Environmental Protection Agency (EPA) list of priority pollutants. The soil and sediment samples were extracted using ultrasonication, and liquid-liquid extraction was utilised for the water samples. Gas chromatography mass spectrometry (GCMS) was used to analyze the PAHs. PAH recoveries ranged between 60 and 110%. The PAH LOD values were between 0.30 and 0.69 μg g-1 and LOQ values ranged between 0.99 and 1.9 μg g-1. The total PAH concentrations determined were between 4.258 and 6.426 μg g-1 in the soil samples, 2.210-13.900 μg g-1 in sediment, and 6.360-85.468 ng L-1 in river water. A comparison between all samples and their respective control, showed that reforestation is potentially reducing the concentration of PAH pollutants. The concentration of pollutants was determined to be lower within the reforestation boundaries and higher outside the reforestation boundary. The total concentration for specific PAHs was above the threshold value for most sampling sites according to Canadian environmental guidelines.

The effects of stir-frying stage and time on the formation of Maillard reaction products (MRP) and potentially hazardous substances with time in stir-fried mutton sao zi were investigated. Furosine, fluorescence intensity, Nε-(1-carboxymethyl)-L-lysine (CML), Nε-(1-carboxyethyl)-L-lysine (CEL), polyaromatic hydrocarbons PAHs), heterocyclic aromatic amines (HAAs), and acrylamides (AA) mainly presented were of stir-fried mutton sao zi. The furosine decreased after mixed stir-frying (MSF) 160 s due to its degradation as the Maillard reaction (MR) progressed. The fluorescent compound gradually increased with time during the stir-frying process. The CML and CEL peaked in MSF at 200 s. AA reached its maximum at MSF 120 s and then decreased. All the 5 HAAs were detected after MSF 200 s, suggesting that stir-frying mutton sao zi was at its best before MSF for 200 s. When stir-frying exceeded the optimal processing time of (MSF 160 s) 200 s, the benzo[a]pyrene peaked at 0.82 μg/kg, far lower than the maximum permissible value specified by the Commission of the European Communities. Extended stir-frying promoted MRP and some hazardous substances, but the content of potentially hazardous substances was still within the safety range for food.

UNASSIGNED: In this study, we aimed to examine the tolerance of mixed culture of microorganisms isolated from sewage waste sludge to degrade high concentrations of polyaromatic hydrocarbons, naphthalene, and phenanthrene. The performance of the artificial neural network (ANN) model to predict and simulate the experimental biodegradation results was investigated.
UNASSIGNED: The mixed culture of microorganisms was isolated from sewage waste sludge and adopted to biodegrade naphthalene and phenanthrene at different concentrations (100-1000mg/L). Sewage waste sludge obtained from wastewater treatment plants. A three-layer feed-forward network with a sigmoid transfer function (logsig) at the hidden layer, a linear transfer function (purelin) at the output layer, and a backpropagation training algorithm was used to set the ANN model.
UNASSIGNED: The results of this study show that naphthalene at concentrations of 100, 300, 700, and 1000 mg/L was depleted after incubation with the mixed culture for 6, 8, 14, and 16 days, respectively. For phenanthrene, depletion of 100, 300, 600, and 1000 mg/L was achieved after 8, 11, 16, and 19 days of incubation, respectively. A high correlation coefficient of 99.5% between the predicted and the experimental results were obtained by using the AAN model.
UNASSIGNED: The results indicated that the mixed culture of microorganisms from sewage waste sludge could effectively consume naphthalene and phenanthrene as carbon and energy sources. Also, the ANN model could efficiently predict the experimental results for biodegradation treatment.

UNASSIGNED: Stormwater is water resulting from precipitation events and snowmelt running off the urban landscape, collecting in storm sewers, and typically being released into receiving water bodies through outfalls with minimal to no treatment. Despite a growing body of evidence observing its deleterious pollution impacts, stormwater management and treatment in cold climates remains limited, partly due to a lack of quality and loading data and modeling parameters. This study examines the quality of stormwater discharging during the summer season in a cold-climate, semi-arid Canadian city (Saskatoon, Saskatchewan).
UNASSIGNED: Seven stormwater outfalls with mixed-land-use urban catchments > 100 km2 were sampled for four summer (June-August 2019) storm events and analyzed for a suite of quality parameters, including total suspended solids (TSS), chemical oxygen demand (COD), dissolved organic carbon (DOC), metals, and targeted polyaromatic hydrocarbons (PAHs). In addition, assessment of stormwater toxicity was done using the two toxicity assays Raphidocelis subcapitata (algae) and Vibrio fischeri (bacteria). Notable single-event, single-outfall contaminant pulses included of arsenic (420 µg/L), cadmium (16.4 µg/L), zinc (924 µg/L), fluorene (4.95 µg/L), benzo[a]pyrene (0.949 µg/L), pyrene (0.934 µg/L), phenanthrene (1.39 µg/L), and anthracene (1.40 µg/L). The IC50 in both R. subcapitata and V. fischeri was observed, if at all, above expected toxicity thresholds for individual contaminant species. Principal component analysis (PCA) showed no clear trends for individual sampling sites or sampling dates. In contrast, parameters were correlated with each other in groups including DOC, COD, TSS, and reduced algal toxicity; and total dissolved solids (TDS), sum of metals, and pH.
UNASSIGNED: In general, stormwater characteristics were similar to those of previous studies, with a bulk of contamination carried by the first volume of runoff, influenced by a combination of rainfall depth, antecedent dry period, land use, and activity within the catchment. Roads, highways, and industrial areas contribute the bulk of estimated contaminant loadings. More intensive sampling strategies are necessary to contextualize stormwater data in the context of contaminant and runoff volume peaks.
UNASSIGNED: The online version contains supplementary material available at 10.1186/s12302-022-00619-x.

Stormwater results from precipitation events and melting snow running off urban landscapes and typically being released into receiving water bodies with little to no treatment. Despite evidence of its deleterious impacts, snowmelt (SM) management and treatment are limited, partly due to a lack of quality and loading data. This study examines snowmelt quality during the spring for a cold climate, semi-arid Canadian city (Saskatoon, Saskatchewan). Four snow storage facilities receiving urban snow plowed from roads in mixed land use urban catchments (228 km2) were sampled including snow piles (five events) and SM (twelve events) runoff in 2019 and 2020. Samples were analyzed for pH, EC, TDS, TSS, COD, DOC, metals, chloride, PAHs, and Raphidocelis subcapitata and Vibrio fischeri toxicity. Notable event-specific TSS spikes occurred on April 13, 2019 (3,513 mg/L), and April 24, 2019 (3,838 mg/L), and TDS, chloride, and manganese on March 26, 2020 (15,000 mg/L, 5,800 mg/L, 574 mg/L), April 17, 2020 (5,200 mg/L, 2,600 mg/L, 882 mg/L), and April 23, 2020 (5,110 mg/L, 2,900 mg/L, 919 mg/L), though chloride remained elevated through May 1, 2020, samples (1,000 mg/L). Additionally, at two sites sampled April 13, 2019, pulses of aluminum (401 mg/L) and PAHs (pyrene, phenanthrene, anthracene; 71 µg/L, 317 µg/L, 182 µg/L) were detected. Concentrations of fluorene, benzo[a]pyrene, pyrene, phenanthrene, and anthracene in almost all SP samples exceeded national aquatic toxicity guideline thresholds, while 50% of SM samples exceeded guideline thresholds for benzo[a]pyrene and pyrene, and almost all exceeded the threshold for anthracene. Nevertheless, the EC50 for R. subcapitata and V. fischeri was observed, if at all, above expected toxicity thresholds.

Exposure to ambient coarse and fine particulate matter (PM10 and PM2.5) causes premature death worldwide due to the nature of their particle size. It contains potentially hazardous elements (PHEs) and polycyclic aromatic hydrocarbons (PAHs). This study aims to quantify the particulate matter (PM) loads on the surface of soil in twenty-five different locations including residential and roadside areas of an urban area in Northeast India. This study shows that the 24h mean concentration of PM (121 ± 49 μg/m3 for PM2.5 and 153 ± 45 μg/m3 for PM10) exceeded more than three times the WHO\'s air quality standard limit for both PM2.5 (25 μg/m3) and PM10 (50 μg/m3) indicating poor air quality in the urban area during monsoon season. The health risk assessment of PAHs and PHEs including mutagenic or carcinogenic potency was observed to be higher as compared to other studies carried out on road traffic emissions in a similar type of urban area. This study also provides a brief database on the deposition of PM on the soil surfaces due to wet-deposition that would help to increase public awareness in such type of urban area for the control of PM pollution and further remediation.

Various separation and mass spectrometric (MS) techniques have furthered our ability to study complex mixtures, and the desire to measure every analyte in a system is of continual interest. For many complex mixtures, such as the total molecular content of a cell, it is becoming apparent that no one single separation technique or analysis is likely to achieve this goal. Therefore, having a variety of tools to measure the complexity of these mixtures is prudent. Orbitrap MSs are broadly used in systems biology studies due to their unique performance characteristics. However, GC-Orbitraps have only recently become available, and instruments that can use gas chromatography (GC) cannot use liquid chromatography (LC) and vice versa. This limits small molecule analyses, such as those that would be employed for metabolomics, lipidomics, or toxicological studies. Thus, a simple, temporary interface was designed for a GC and Thermo Scientific™ Ion Max housing unit. This interface enables either GC or LC separation to be used on the same MS, an Exactive™ Plus Orbitrap, and utilizes an atmospheric pressure chemical ionization (APCI) source. The GC-APCI interface was tested against a commercially available atmospheric pressure photoionization (APPI) interface for three types of analytes that span the breadth of typical GC analyses: fatty acid methyl esters (FAMEs), polyaromatic hydrocarbons (PAHs), and saturated hydrocarbons. The GC-APCI-Orbitrap had similar or improved performance to the APPI and other reported methods in that it had a lower limit of quantitation, better signal to noise, and lower tendency to fragment analytes.